Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_provenance.
- NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_assertion description "[In SCA2 patients, one patient exhibited MSA-P phenotype, and the other five exhibited ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_provenance.
- NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_assertion evidence source_evidence_literature NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_provenance.
- NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_assertion SIO_000772 21334959 NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_provenance.
- NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_assertion wasDerivedFrom befree-20150227 NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_provenance.
- NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_assertion wasGeneratedBy ECO_0000203 NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP756695.RABsMO7V27RED50I5VFUUpxgKgEwdTR_aodUE2Vhpr1x4130_provenance.